Biotherapeutic Analytics Scientist - Large Molecules

Eurofins; Chesterfield (MO); On-site; USD 85,000 - 110,000; Full time

Job summary

Eurofins USA PSS Insourcing Solutions is seeking an Analytical Scientist to support biotherapeutic process development, focusing on large molecule characterization. You will develop and execute analytical methods to enable process understanding and product quality assessment across development stages.

The role requires hands-on CGE, qPCR, and HPLC, with SEC-MALS valued. A BS/MS in a related field plus 3–5 years of experience is expected; US work authorization is required.

Qualifications

• Required hands-on experience with CGE, qPCR, and HPLC.
• Experience with SEC-MALS is strongly valued.
• Bachelor’s or Master’s degree in a related scientific discipline.
• 3–5 years of relevant industry experience in a lab or biotherapeutic development environment.
• Authorization to work in the United States without sponsorship.
• Commutable distance to Chesterfield, MO is encouraged.

Responsibilities

• Provide hands-on analytical support for biotherapeutic process development teams.
• Perform and optimize analytical assays for large molecule characterization.
• Analyze and interpret data, ensuring accuracy and alignment with project goals.
• Collaborate cross-functionally with process development, quality, and project teams.
• Maintain clear and detailed documentation in accordance with regulatory and quality standards.
• Support troubleshooting and continuous improvement of analytical methods.

Skills

CGE (Capillary Gel Electrophoresis)

qPCR

HPLC

Large molecule characterization

Data analysis

Education

Bachelor’s or Master’s degree in Biotechnology/Analytical Chemistry/Biochemical Engineering/Chemical Engineering

Tools

ELN systems

GMP documentation practices

Empower/OpenLab software

Job description

Eurofins USA PSS Insourcing Solutions is seeking an Analytical Scientist to support biotherapeutic process development, focusing on large molecule characterization. You will develop and execute analytical methods to enable process understanding and product quality assessment across development stages.

The role requires hands-on CGE, qPCR, and HPLC, with SEC-MALS valued. A BS/MS in a related field plus 3–5 years of experience is expected; US work authorization is required.